Canonical Allele Identifier: CA2324923117

Gene: CYP4F22

Linked Data

• dbSNP Id: rs997773654

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15529636G>T , CM000681.2:g.15529636G>T	GRCh38
NC_000019.9:g.15640447G>T , CM000681.1:g.15640447G>T	GRCh37
NC_000019.8:g.15501447G>T	NCBI36
NG_007987.1:g.26112G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269703.8:c.223-73G>T MANE Select	ENSP00000269703.1:n.223-73G>T
ENST00000269703.7:c.223-73G>T	ENSP00000269703.1:n.223-73G>T
ENST00000601005.2:c.223-73G>T	ENSP00000469866.1:n.223-73G>T
NM_173483.3:c.223-73G>T	NP_775754.2:n.223-73G>T
XM_011527692.1:c.223-73G>T	XP_011525994.1:n.223-73G>T
XM_011527693.1:c.223-73G>T	XP_011525995.1:n.223-73G>T
XM_011527692.2:c.223-73G>T	XP_011525994.1:n.223-73G>T
XM_011527693.2:c.223-73G>T	XP_011525995.1:n.223-73G>T
NM_173483.4:c.223-73G>T MANE Select	NP_775754.2:n.223-73G>T